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Would you like to be part of driving and setting the direction for the health agenda in Arla Foods?
Spend a year in this maternity cover in a highly skilled team of scientists based in our brand-new innovation centre. And gain a network across the organisation as you work cross-functionally and with different science teams.
In this maternity cover, starting as soon as possible, you will get to play an important role in ensuring our Arla products are as healthy and innovative as possible. Thus, you will be the primary point of contact for the cheese and butter categories and for our markets in the Middle East .
Bioneer A/S, Hørsholm
Bioneer A/S søger en laborant med molekylær- og cellebiologisk erfaring, samt med kendskab til arbejde med bakterier.
Er du interesseret i varierende arbejdsopgaver inden for molekylærbiologi og rekombinant DNA teknologi samt dyrkning af mammalle celler og bakterier? Så kan det være, du er vores nye kollega i Bioneer A/S.
Som laborant vil du arbejde med molekylærbiologi, herunder specielt anvendelse af teknikker indenfor rekombinant DNA teknologi (f. eks vektorkonstruktion, PCR og gen-editering) i både mammalle og bakterielle systemer. Arbejdet vil også indebære dyrkning og håndtering af både mammalle celler og bakterier med fokus på fremstilling af rekombinante cellelinjer eller bakterier. Derudover vil du skulle indgå i opgaver med opsætning af in vitro assays, som kan inkludere flow cytometri og ELISA.
Quantitative Modelling of Cell Metabolism (QMCM) is a new section at the Novo Nordisk Foundation Center for Biosustainability (DTU Biosustain).
In QMCM, we focus on developing mathematical models to explore and explain the molecular basis for homeostasis – the self-regulating processes evolved to maintain metabolic equilibrium in organisms.
The successful candidate will be primarily responsible for providing high-throughput quantitative metabolomics analyses to biological researchers. Assays will include targeted metabolomics and flux analysis using both LC-MS and GC-MS. The successful candidate will be involved in communicating with users, participation in experimental design, sample preparation, Instrument analysis, data interpretation, and instrument management.
Novo Nordisk A/S, Bagsværd
Do you like to be a driving force in ensuring highest safety and lowest possible risk to patients that use liraglutide? And would you like to be part of one of the most skilled and advanced safety functions in Denmark?
You will be primarily responsible for signal detection and management which includes the critical analysis and medical evaluation of the emerging safety data from clinical trials, marketed use, published literature and regulatory databases. You will be responsible for understanding the product safety profile and developing and maintaining the reference safety information and the labelling for Novo Nordisk products. You will also be responsible for communication about the benefit risk assessment (Periodic Safety Update Report (PSUR), Development Safety Update Report (DSUR) and Risk Management Plan (RMP) and you will be our safety representative in cross-functional teams.
UNICEF Supply Division, Nordhavn
Would you like to be part of the dynamic team who manages the nutrition and medicines product supply for children of the world most in need? UNICEF Supply Division Copenhagen is seeking a highly motivated individual to assist with the quality assessment of strategic nutrition products that are distributed globally.
- Reviews the technical documentation provided by suppliers in response to unit bidding activities, prepares a technical evaluation summary report for approval by the Technical Specialist.
- Conducts sample evaluation as part of the technical evaluation process if necessary.
- Drafts, prepares and finalizes product specifications for UNICEF Supply Division’s nutrition products on basis of existing documentation, directives and customer requirements. Translates specifications with expert help if necessary.
We are looking for very talented PhD organic chemists with a strong background in synthetic organic chemistry to work at our small-scale development site in Lumsås, Nordvestsjælland, approximately 35-40 min from Roskilde.
The position is in our Safety and Technical Chemistry group in Lumsås and is part of the Process Chemistry group. It is responsible for the supply of multi-Kg amounts of development candidates to support investigational and clinical studies.
Your job and key responsibilities
Development, optimisation and the scale up of chemical processes to enable multi-kg amounts of development compounds to be produced safely under full GMP on time to support clinical studies. Further development of chemical processes already implemented in process development and design of 2nd generation synthetic procedures
We are seeking a highly motivated and expert medicinal chemist to join the department of Medicinal Chemistry. As an outstanding medicinal chemist with documented results, you can become an integral member of a world-class medicinal chemistry team and help to drive innovation in small molecule drug discovery and join our quest for new medicines to treat Central Nervous System (CNS) diseases.
As a Principal Scientist in Medicinal Chemistry you will be involved in all aspects of the medicinal chemistry value chain, and expected to provide scientific oversight and accept accountability of medicinal chemistry activities in assigned projects. You will be expected to manage a multi-disciplinary team of scientists within ongoing hit to tool and lead optimization projects and promote a culture that embraces open scientific debate and agile, accountable decision-making.
Coloplast A/S, Humlebæk
At the Coloplast Global R&D organization in Humlebæk, Denmark, you join a development team of 24 colleagues. We are a mixed team consisting of scientists with biological as well as polymer chemistry backgrounds, technicians and a nurse. We support product and technology development projects with the best test methods solutions. We seek a colleague with a passion for investigating behavior of medical devices with our end users and developing test methods based on this.
As a Pre-Clinical test method scientist, you develop new test methods based on a deep understanding of how devices work together with our users and the challenges in the user situations. Beside working together with your colleagues in the pre-clinical team you will also work closely together with material and mechanical design specialist as well as users of our products.
The focus of The Novo Nordisk Foundation Center for Biosustainability (DTU Biosustain) is to develop cell factories for producing chemicals and other products in a sustainable way. The list of things that can be made by engineered cell factories includes biofuels, bioplastics, drugs, food supplements and much more.
We are looking for an enthusiastic and skilled data scientist for The Novo Nordisk Foundation Center for Biosustainability (DTU Biosustain). This person will be part of the Data Science and Automation Unit of the Center and will work closely with both technical teams (software engineering, data management, other data scientists) and with application-oriented teams working on developing cell factories for sustainable production of chemicals and proteins.
Siemens Healthcare AS, Ballerup
We are looking for a bright mind eager to join a dynamic and highly motivated team, in which you will work closely with colleagues from Sales, Customer Service, and Project Management among others. You will work towards establishing closer cooperation between Siemens Healthineers and our customers, and be a part of our continuous efforts to strengthen our relations with our customers in Denmark and the Nordic countries.
As MR Physicist in Siemens Healthineers in Denmark it will be your responsibility to maintain a good and close collaboration with the leading hospitals in Denmark within MR research and innovation. Your main responsibilities will be to:
- Deliver high-end MR application support to our customers
- Offer support to research and innovation projects at the hospitals
- Prepare and implement Master Research Agreements (MRA) with leading hospitals in Denmark
Curia recruiting on behalf of Tracer Pharma Aps in Hørsholm
Can you plan and lead all production deliverables and do you want to have a key role in a global collaboration environment?
racer Pharma Aps develop and manufacture Active Pharmaceutical Ingredients (API’s) for vitro diagnostic kits, in combination with human drugs, for pharmaceutical and med tech use. The core products are distributed in Europe and the customers are leading players within their field of business.
With reference to the General Manager, your primary tasks are:
- Planning and leading all production deliverables, including day-to-day operations.
- Chemical synthesis production of API’s under GMP and secure all necessary documentation and other production relevant necessities to support the release of the API’s. In collaboration with the QA Manager, and your team members in the production.
Coloplast A/S, Humlebæk
At the Coloplast Global R&D organisation in Humlebæk, Denmark, you join a development team of 24 colleagues. We are a mixed team consisting of scientists with biological as well as polymer chemistry backgrounds, technicians and a nurse. We support product and technology development projects with the best test methods solutions. We seek a colleague with a passion for investigating behavior of medical devices with our end users and developing test methods based on this.
As a microbiologist, you develop new test methods based on a deep understanding of how devices work together with our users and the challenges in the user situations. Beside working together with your colleagues in the pre-clinical team, you will also work closely together with material scientist and mechanical design specialist as well as users of our products.
Chr. Hansen A/S, Hørsholm
This position works under limited direction and is primarily responsible for the understanding and application of food cultures and enzymes, primarily into the cheese and fermented milks industry.
Principal Duties And Responsibilities
- Conducts field evaluations and demonstrations of new ingredient systems in conjunction with Global Innovation including Application Centers. Completes written reports, including conclusions and develops follow-up plans as required in a timely manner. Maintains accurate visit reports, records and files in the required databases.
- Provides customer support for product application by plant visits, audits and trouble-shooting issues.
- Conducts technical presentations to customers, explaining the use of CH ingredient systems in food applications. Organizes and provides training programs for customers and/or industry trade groups and participates in industry and company technical meetings.
Carlsberg Breweries A/S, Copenhagen
Carlsberg A/S has one opening for a two-year Project Scientist position to work with abiotic stress in the Raw materials Group at the Carlsberg Research Laboratory (CRL).
As Project Scientist you will:
- Be part of a team breeding barley for the future.
- Participate with and interact in a project group consisting of Carlsberg Research Laboratory and world leading academic partners.
- Work on mineral transporters involved in soil-plant uptake and transport within the plant
You will be part of a world leading global company that provides an experienced international team and excellent research facilities. Our research group applies a range of technologies and advanced approaches in developing the future elite barley.
Novozymes A/S, Bagsværd
As an application scientist, you will be responsible for leading enzyme development projects, many of which are conducted in collaboration with customers. Your technical responsibilities will include assay development, enzyme screening and application testing of enzyme product candidates. In addition to your creativity in the early project phases, we need persistence and drive to see the complex projects through to launch.
In this position you need:
- A strong scientific background (PhD or MSc level) in biochemistry, microbiology, environmental science, chemical engineering or the like
- Practical experience in applied science, preferably related to enzymes, and knowledge of detergent formulations
- The ability to understand the business and the consumer needs
Novozymes A/S, Bagsværd
We are looking for a new Zymer to join our dedicated, small team that focuses on ensuring safety of Novozymes microbial products. Our tasks consist of supporting research and sales departments in assessing Novozymes innovative products to ensure that products are safe in handling and use.
As every day is different from the previous, it is essential to us to take care of each other and support a good working environment. You will become a member of a dedicated and competent group of people comprising 35 employees split in two departments; Toxicology & Immunology and Application Safety. We work closely together with our Regulatory function, which operate globally.
Do you have solid experience with Research & Development tasks in E&P business and a strong track record within technical execution of development or research projects? Then you might be the production chemistry advisor that we are looking for at DHRTC.
You will be part of the Technology Maturation group, which is responsible for the technical integration of the research results and for technical support to the partnership research community and DHRTC Programme Management.
It will be your responsibility to develop and maintain technology demonstration models, within your area of expertise. Demonstration models are directed towards integrating various areas of research into applicable and commercially viable solutions with high impact for the oil & gas production in the North Sea.
Gubra ApS, Hørsholm
At Gubra we are looking for a talented and dedicated research scientist for our NASH-histopathology group. The priority of the group is to deliver high quality histological data in an efficient manner within NASH/NAFLD, diabetes, obesity and related metabolic disorders.
We are looking for a competent scientist with great histological skills and biological understanding; a colleague who can navigate and collaborate in an energetic organization and help drive our research activities forward.
Your tasks as a Histology Research Scientist are varied, but will include:
- Conduction of internal discovery and external contract research activities
- Pathological/histological scoring and quantitative analysis of liver sections
- Coordinating and supporting experiments in the laboratory
Coloplast A/S, Humlebæk
Use your technical insight to bring new, advanced wound and skin care products to market – and join a team of commercially savvy colleagues who bridge science, innovation and documentation to improve the standards of wound and skin care globally.
Navigating an increasingly challenging regulatory landscape, you will produce documentation which meet the latest requirements from relevant authorities in the global market. Collaborating cross-functionally, you will tie together knowledge from across our organisation as it is your responsibility to plan and drive the design control and risk management activities for our wound care innovation projects.
Your main responsibility will be to write and review documentation to support regulatory files, and you will be responsible for ensuring that relevant product standards are met.
Unique Human Capital recruiting on behalf of a client in Copenhagen
Challenging position in an exciting biotech company
As Clinical Trial Administrator (CTA) you will join a dedicated team of professionals and become an important part of the Clinical Development staff of a progressive and innovative Danish biopharmaceutical company with a late stage pipeline. The company is based in Copenhagen and you will have direct report to VP Clinical Operations.
The position is newly established, and you will support the Clinical Operations Team in the day to day conduct of clinical trials. Primary responsibilities include tracking and maintenance of clinical trial documentation associated with the conduct of investigational clinical trials in accordance with FDA regulations, Good Clinical Practice (GCP), and company Standard Operating Procedures (SOPs).